TRIUM is not your typical CRO but rather an expert clinical solutions provider.
It’s a unique combination of global CRO services, staffing/resourcing solutions incl. search& selection, quality consultancy, GDPR and risk-based approaches consultancy and training services.
It is our mission to be a passionate, dedicated business partner with a focus on excellence to provide an encompassing range of services.
Our CRO services cover the full spectrum of clinical trial activities, ranging from initial concept development, regulatory strategy, protocol development, medical writing, vendor management, risk-based strategies, feasibility, site/investigator selection, site start‐up including ethics committee and competent authority submissions, site management including on‐site or remote (risk-based) monitoring, data management, biostatistics, e-solutions, EDC, IXRS, lab and core lab services, safety, medical monitoring and CEC/DSMB services, all on a global level.
In addition, we provide global flexible staffing solutions and tailored search & selection for the medical device, biotech and pharma field covering any role, function or therapeutic area, remote or office-based support, individuals or teams on an FTE or project basis for short or long durations.
We also offer quality assurance (QA) and quality control (QC) services (GDPR services, audits, audit/inspection readiness, risk-based approaches, QMS setup and maintenance, root cause analysis and CAPA, SOP writing and review, ...)
Lastly, we specialize in performance and competency-based clinical research training. Next to clinical research regulations, standards and guidelines, we offer training on specific clinical research skills as well as applicable soft- and line-management skills.
Our full training portfolio is available on https://www.triumclinicalconsulting.com/training-services/